Disitamab Vedotin + Pyrotinib Versus THP in the First-line Treatment for HER2+ Advanced Breast Cancer Clinical Trial

Inclusion Criteria:

1. Adult female patients (age 18-75 years) with metastatic breast cancer confirmed bypathology or imaging;
2. Pathologically confirmed HER2 positive (definition: Immunohistochemistry(IHC) 3+, orIHC 2+ and Fluorescent In Situ Hybridization(FISH) amplification);
3. No previous chemotherapy regimen for metastatic breast cancer;
4. At least one measurable lesion exists (Response Evaluation Criteria in SolidTumors(RECIST) 1.1);
5. Eastern Cooperative Oncology Group(ECOG) performance status score ≤ 2 and expectedsurvival of not less than 3 months;
6. Prior treatment-related toxicity at enrollment must have resolved to National CancerInstitute(NCI) Common Terminology Criteria for Adverse Events(CTCAE) (version 5.0) ≤ 1degree (except for alopecia or other toxicity that, in the judgment of theinvestigator, is not considered a risk to the safety of the patient);
7. Patients with adequate organ function before enrollment:
8. White Blood Cell (WBC) ≥ 3.0 x 10^9/L;
9. Neutrophil granulocyte (ANC) ≥1.5 x 10^9/L;
10. Platelet (PLT) ≥70×10^9/L;
11. Liver, kidney, and cardiac function tests are essentially normal (based on the normalvalues in the laboratory of each study center):
12. Total bilirubin (TBIL) ≤ 3 x Upper Limit of Normal (ULN);
13. Alanine aminotransferase (ALT/AST) ≤ 2.5 x ULN (≤ 5 x ULN in patients with livermetastases);
14. serum creatinine ≤ 1.5 x ULN or creatinine clearance (Ccr) ≥ 60 ml/min;
15. . Normal cardiac function;
16. Left ventricular ejection fraction (LVEF) ≥ 55%;
17. QT-interval corrected with Fridericia (QTcF) ≤ 470ms;
18. Hormone receptor status is clear;
19. Female patients of childbearing potential who have a negative pregnancy test and agreeto use an effective non-hormonal method of contraception during treatment and for atleast 6 months after the last dose of the test drug;
20. Able to understand the study process, voluntarily participate in this study, and signan informed consent form.

Exclusion Criteria:

1. Pathology suggestive of HER2 negativity (IHC 2+ and FISH-, or IHC 1+);
2. Patients with known hypersensitivity to the active ingredient or other components ofthe study drug;
3. Patients during pregnancy or lactation, patients with childbearing potential testedpositive in a baseline pregnancy test, or patients unwilling to take effectivecontraceptive measures throughout the trial;
4. Patients not eligible for this study judged by the investigator, a pre-existingdisease or condition that may interfere with participation in the study or any seriousmedical disorder that may interfere with the safety of the subject (e.g., uncontrolledheart disease, high blood pressure, active or uncontrolled infections, activehepatitis B virus infection).